[go: up one dir, main page]

EP2658510B2 - Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels - Google Patents

Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels Download PDF

Info

Publication number
EP2658510B2
EP2658510B2 EP11807932.6A EP11807932A EP2658510B2 EP 2658510 B2 EP2658510 B2 EP 2658510B2 EP 11807932 A EP11807932 A EP 11807932A EP 2658510 B2 EP2658510 B2 EP 2658510B2
Authority
EP
European Patent Office
Prior art keywords
composition
bleaching
composition according
polyquaternium
hair
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP11807932.6A
Other languages
German (de)
English (en)
Other versions
EP2658510A1 (fr
EP2658510B1 (fr
Inventor
Jonathan Wood
Anja AECHTRNER
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Germany GmbH
Original Assignee
Kao Germany GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43901574&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2658510(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kao Germany GmbH filed Critical Kao Germany GmbH
Priority to EP11807932.6A priority Critical patent/EP2658510B2/fr
Publication of EP2658510A1 publication Critical patent/EP2658510A1/fr
Publication of EP2658510B1 publication Critical patent/EP2658510B1/fr
Application granted granted Critical
Publication of EP2658510B2 publication Critical patent/EP2658510B2/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365Hydroxycarboxylic acids; Ketocarboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/22Peroxides; Oxygen; Ozone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/23Sulfur; Selenium; Tellurium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/08Preparations for bleaching the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/51Chelating agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88Two- or multipart kits
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88Two- or multipart kits
    • A61K2800/882Mixing prior to application

Definitions

  • the present invention relates to bleaching composition for keratin fibres, especially human hair, comprising at least one compound with bleaching and/or highlighting effect and a specific chelating agent.
  • Hair bleaching is a common practice for ages. It is based on oxidative decomposition of hair colour, which is usually done using peroxide or peroxide releasing compounds such as persulfates. Due to highly irritating potential of these bleaching ingredients and dustiness of powder compositions, it is preferred to provide granular composition where dust is reduced by agglomerating small particles into granulates using various binding agents. Most popular binding agent is mineral oil, which was the subject matter of EP 560 088 B1 . Furthermore, EP 778 020 A1 suggests the use of oil and wax compounds or their mixtures for preparation of suspensions.
  • the bleaching of human hair customarily consists of a process with the following steps: Homogenous mixing of a water-free preparation, preferably a powder, comprising at least one compound with a bleaching and/or highlighting effect, in particular a solid peroxide salt, preferably ammonium, potassium and/or sodium persulfate or earth alkali peroxide, with an aqueous hydrogen peroxide composition, application of this composition onto the hair, and rinsing after bleaching is completed.
  • a water-free preparation preferably a powder
  • a bleaching and/or highlighting effect in particular a solid peroxide salt, preferably ammonium, potassium and/or sodium persulfate or earth alkali peroxide
  • aim of the present invention is to find out a composition for bleaching and/or highlighting hair which does effectively bleach hair but causes less damage so that repeated bleaching processes may be done without causing ultimate hair loss.
  • a bleaching composition based at least one compound with bleaching effect and furthermore comprising a specific chelating agent effectively bleaches hair and causes less hair damage.
  • the first object of the present invention is a substantially water free bleaching and/or highlighting composition for keratin fibres, especially human hair, comprising at least one compound with bleaching and/or highlighting effect at a concentration of at least 5% by weight, calculated to total composition, and gluconic acid and/or its salts as a chelating agent, whereby compositions consisting of sodium citrate (15-30%), sodium silicate (15-30%), sodium percarbonate (15-30%), sodium carbonate (5-15%), sodium gluconate (5-15%) and non ionic vegetal surfactants ( ⁇ 5%) are excluded from the scope.
  • the second object of the present invention is the use of a substantially water free composition comprising at least one compound with bleaching and/or highlighting effect at a concentration of at least 5% by weight, calculated to total composition, and gluconic acid and/or its salts as a chelating agent for effectively bleaching keratin fibres especially human hair.
  • bleaching composition is used to define any bleaching composition either water free or an aqueous i.e. after mixing with aqueous oxidizing agent.
  • substantially water free bleaching and/or highlighting composition it is meant that no additional water is introduced into the composition other than bound water which may be as high as 1% of the composition.
  • the composition comprises at least one compound with bleaching and/or highlighting effect.
  • Suitable compounds are in general peroxides.
  • Useful as such are in particular persulfates such as sodium and potassium persulfate, ammonium persulfate, earth alkali peroxides such as magnesium peroxide, melamine peroxide or urea peroxide or phtholimidoperoxyhexanoic acid, and mixtures thereof.
  • the proportion of peroxides is at least 5%, preferably in the range of 20 to 80%, more preferably 25 to 60% and most preferably 30 to 55% by weight, calculated to total composition prior to mixing with oxidizing lotion.
  • the substantially water free composition can also comprise 0.1% to 10% by weight, calculated to total composition prior to mixing with oxidizing lotion, at least one ammonium salts.
  • Suitable ammonium salts are ammonium carbonate, ammonium hydrogen carbonate, ammonium carbamate, ammonium chloride, ammonium sulfate, ammonium phosphates, ammonium nitrate, ammonium bromide, ammonium iodide, ammonium thiosulfate, ammonium molybdate, ammonium vanadate, ammonium sulfamate, ammonium citrate, ammonium salicylate, ammonium valerate, ammonium tartarate, ammonium benzoate, ammonium acetate, ammonium formiate and ammonium lactate.
  • Compositions may also comprise mixture or ammonium salts.
  • ammonium phosphates such as ammonium dihydrogen phosphate, ammonium hydrogen phosphate, diammonium sodium phosphate, sodium ammonium hydrogen phospahe, ammonium disodium phosphate, as well as ammonium chloride, ammonium sulphate, diammonium hydrogen citrate, ammonium carbonate, ammonium hydrogen carbonate preferably in an amount from 0.1% to 10% by weight, calculated to total composition prior to mixing with oxidizing lotion.
  • Composition of the present invention comprises gluconic acid and/or its salts especially mono valent cation salts such as sodium, potassium and ammonium salts.
  • Concentration of gluconic acid and/or its salts may be in the range of 0.01 to 10%, preferably 0.05 to 7.5% and more preferably 0.1 to 5% and most preferably 0.1 to 4% by weight calculated to total of the composition.
  • substantially water free bleaching and highlighting composition of the present invention is in powder form and in particular in dust free powder form and comprises oily lipophilic ingredients such as vegetable oils, for example, jojoba oil or any other; petrolatum liquid paraffins, especially paraffinum perliquidum and parafiinum subliquidum; silicone oils; hydropobic fatty acid esters such as octyl palmitate, isocetyl palmitate, isopropyl palmitate and octyl stearate, C 10 - to C 36 -fatty acid triglycerides, as well as their mixtures.
  • vegetable oils for example, jojoba oil or any other
  • petrolatum liquid paraffins especially paraffinum perliquidum and parafiinum subliquidum
  • silicone oils hydropobic fatty acid esters such as octyl palmitate, isocetyl palmitate, isopropyl palmitate and octyl stearate, C 10 - to C 36 -fatty acid t
  • silicone oils In the case that the use is wished among those the most preferred ones are silicone oils, jojoba oil, fatty acid esters, paraffin oils, combinations of fatty acid esters and paraffin oils. Fatty acid esters and/or paraffin oils and/or silicone oils are particularly preferred. Concentration of these oily lipophilic compounds may be used in a total amount of about 0.1 to 50% by weight, preferably 0.5 to 40%, more preferably 1 to 35% and most preferably 2.5 to 30% by weight, calculated to total composition prior to mixing with oxidizing lotion.
  • any silicone oil is useful as a lipophilic compound.
  • Non-limiting suitable examples are dimethicones with various viscosity available from Dow Corning under the trade name DC 200, arylated silicones such as phenyl methicone, phenyl trimethicone, diphenyl dimethicone, diphenylsiloxy phenyl trimethicone, tetramethyl tetraphenyl trisiloxane, triphenyl trimethicone, tetramethly tetraphenyl trisiloxane and pentaphenyl trimethyl trisiloxane.
  • arylated silicones such as phenyl methicone, phenyl trimethicone, diphenyl dimethicone, diphenylsiloxy phenyl trimethicone, tetramethyl tetraphenyl trisiloxane, triphenyl trimethicone, tetramethly tetraphenyl trisiloxane and
  • substantially water free composition for bleaching and/or highlighting hair comprises polymers from the group consisting of cellulose polymer compounds, alginate, polysaccarides and acrylic acid polymers, preferably methyl cellulose compounds, ethyl cellulose compounds, hydroxyethylcellulose compounds, methylhydroxyethylcellulose compounds, methylhydroxypropylcellulose compounds, carboxymethyl cellulose compounds, alginic acids, sodium alginates, ammonium alginates, calcium alginates, gum arabic, guar gum or xanthan gum, or acrylic acid polymers with molecular weights from about 1,250,000 to 4,000,000, alone or in combination with each other.
  • the polymers may be used in a total amount of 0.1 to 15 %, preferably from 0.2 to 10 %, and more preferably in an amount of from 0.5 to 7.5% by weight, calculated to total composition prior to mixing with oxidizing lotion.
  • Substantially water free bleaching and/or highlighting composition can also comprise cationic polymers as conditioning and/or thickening agents.
  • cationic polymers know as Polymer JR type from Amerchol such as Polyquaternium 10 or cationic guar gum known with trade name Jaguar from Rhône-Poulenc and chemically for example Guar hydroxypropyl trimonium chloride.
  • chitosan and chitin can also be included in the compositions as cationic natural polymers.
  • Typical concentration range for any of the cationic conditioners mentioned above can be 0.1 - 7.5% by weight, preferably 0.3 - 5% by weight and more preferably 0.5 - 2.5% by weight, calculated to total composition prior to mixing with an oxidizing agent.
  • Substantially water free bleaching and/or highlighting composition of the present invention may comprise at least one dialkyl carbonate of general formula R 30 OC(O)OR 31 where R 30 and R 31 are independent from each other linear or branched saturated alkyl chains with 6 to 22 C atoms.
  • Preferred at least one dialkyl carbonate is selected from di(caprylyl) carbonate and di(ethylhexyl) carbonate.
  • Concentration of at least dialkyl carbonate may vary between 0.1 and 30% by weight calculated to total composition prior to mixing with an oxidizing agent.
  • Substantially water free bleaching and/or highlighting compositions of the present invention can comprise synthetic mica coated with metal oxide or oxides having a volume particle size distribution in the range of 1 to 750 ⁇ m.
  • Use of synthetic mica coated with metal oxide or oxides mainly in decorative cosmetics is disclosed in an international patent application of Sun Chemical Corporation published with a number WO 2005/065632 A1 .
  • synthetic mica and coated synthetic mica with at least one metal oxide or oxides is disclosed in detail. The content of the document is included herewith by reference.
  • Suitable metal oxide or oxides for coating synthetic mica are titanium dioxide, chromium oxide, ferric oxide or mixtures thereof.
  • the preferred is synthetic mica coated with titanium dioxide.
  • Such materials are commercially available from Sun Chemical Corporation and Merck (Timiron Synwhite 40) and known with their INCI names Synthetic Fluorphologopite
  • the volume particle size distribution of synthetic mica coated with a metal oxide or oxides is in the range of 1 to 750 ⁇ m, preferably 1 to 250 ⁇ m, more preferably 1 to 100 ⁇ m and most preferably 5 to 95 ⁇ m.
  • the particle sizes referred are relating to the volume particle size distribution meaning that particles found in the coated synthetic mica having volume particle size in the given ranges.
  • Concentration of synthetic mica coated with at least metal oxide or oxides may be from 0.01 to 20%, preferably 0.1 to 15%, more preferably 0.25 to 10% and most preferably 0.5 to 55% by weight calculated to total composition prior to mixing with an oxidizing agent.
  • the mixture of substantially water free powder composition comprising at least one bleaching and/or highlighting agent, at least one magnesium salt and synthetic mica coated with at least one metal oxide or oxides with a particle size as mentioned above and a composition comprising at least one oxidizing agent look very homogeneous, shiny and easy to apply onto hair than a mixture which does not comprise synthetic mica.
  • the average particle size of the dust free bleaching powder composition according to the invention is generally range below 1 mm, preferably below 500 ⁇ m, more preferably less than 400 ⁇ m and in particular about 25 to about 100 ⁇ m, thus ensuring excellent processing capability, i.e. miscibility with an aqueous hydrogen peroxide solution prior to application onto human hair.
  • Bleaching and/or highlighting compositions of the present invention may comprise one or more magnesium and/or calcium salt in order to prevent heating up and/or foaming when mixed with an aqueous composition comprising at least one oxidizing agent.
  • magnesium salts are magnesium aluminium borosilicate, magnesium aspartate, magnesium borate, magnesium bromate, magnesium bromide, magnesium benzoate, magnesium acetate, magnesium carbonate, magnesium citrate, magnesium clorate, magnesium dihydrogen phosphate, magnesium fluoride, magnesium formate, magnesium hydroxide, magnesium iodide, magnesium lactate, magnesium mandalate, magnesium monofluorophosphate, magnesium oxalate, magnesium oxide, magnesium perborate, magnesium phosphate, magnesium propionate, magnesium pyrophosphate, magnesium salicylate, magnesium silicate, and magnesium tartarate.
  • Concentration of diamide compounds in the compositions of the present invention may be in the range of 0.001 to 5%, preferably 0.002 to 3% more preferably 0.005 to 2% and most preferably 0.01 to 1% by weight calculated to total composition.
  • the powder composition can be produced with processes such as by mixing the powdery ingredients first and subsequently adding lipophilic ingredient(s) and by fluidized bed method.
  • fluidized bed method powder ingredients are mixed in a vessel and made flowing by inletting an air flow which may be heated (preferred when using waxy component) or carried out at room (ambient) temperature and while the powder mix freely "flowing" lipophilic ingredinet and/or mixture with any other liquid component is sprayed from a nozzle mounted above the powder batch.
  • the bleaching and/or highlighting composition of the present invention is mixed prior to application with an oxidizing lotion comprising at least one oxidizing agent.
  • the oxidizing agents suitable are hydrogen peroxide, urea peroxide, melamin peroxide or perborate salts. The most preferred is hydrogen peroxide.
  • Such composition comprises 2 to 12% by weight at least one oxidizing agent preferably hydrogen peroxide and is either a solution or in the form of an emulsion.
  • the mixing ratio is very much dependent on the level of bleaching effect targeted, i.e. the level of highlighting and/or bleaching and darkness of hair before bleaching, and can be adjusted accordingly by hair dressers. However, generally mixing ratio is within the range of 0.5 to 4 by weight (bleaching composition to oxidizing composition), preferably in the range of 1 to 2 by weight.
  • the pH of the ready to use product, mixture of bleaching composition and oxidizing lotion is in the range of 8 to 12, in particular between 9 and 11.
  • a third composition is mixed into the mixture of water free bleaching and/or highlighting composition and oxidizing composition.
  • the third composition is preferably an aqueous composition and can be in form of a solution, thickened composition, gel, emulsion or a suspension. It may even be a product dispensed from a pressurised contained including any one of the above mentioned type of preparations.
  • the third composition preferably comprises at least one hair conditioning compound.
  • Hair conditioning compound is preferably selected from non-ionic substances, oil or oily substances, cationic compounds.
  • Non-ionic conditioning agents can be polyethyleneglycol mono or di fatty acid esters having general formula R 4 CO(OCH 2 CH 2 ) n OH or R 4 CO(OCH 2 CH 2 ) n OOCR 5 wherein R 4 and R 5 are independent from each other saturated, unsaturated or branched or non-branched alkyl chain with 7 to 21 C atoms and n is typically 2 - 100.
  • Suitable cationic conditioning compounds are those carrying a quaternary ammonium group or a cationizable group and selected from cationic polymers, cationic surfactants and quaternary ammonium or amino silicones.
  • Suitable cationic polymers are those of best known with their CTFA category name Polyquaternium as disclosed above for water free bleaching and/or highlighting composition as well as those polymers known with their CTFA category name Quaternium and disclosed above for water free bleaching and/or highlighting composition.
  • the third composition and also water free bleaching composition of the present invention can comprise an organopolysiloxane wherein at least one silicium atom is linked to an alkylene group having a hetero-atom, in particular a nitrogen atom, with a poly-(N-acyl alkyleneimine) units of the formula wherein n is a number from 1 to 5 and R 6 is hydrogen, a C 1 -C 12 -alkyl or cycloalkyl, aralkyl or aryl group as a conditioning agent.
  • Preferred organopolysiloxane polymers are those of the type disclosed in EP-A 640 643 , in particular optionally quaternized aminoalkyl, in particular aminopropyl dimethyl polysiloxane/polyethyl oxazoline copolymers of the formula wherein m and n each are numbers from 20 to 10,000, in particular 50 to 7,000, especially 100 to 5,000, x is a number between 1 and 5, preferably 3, and y is a number from 5 to 30, R 7 is a C 1 -C 12 -alkyl or aryl group, in particular a methyl, ethyl or benzyl group, and Y - is an anion.
  • the proportion of graft copolymers in the hair colouring compositions according to the invention ranges from 0.05% to 5%, preferably 0.1 % to 2.5%, in particular 0.5% to 1.5% by weight, calculated to the total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • Cationic surfactants suitable for the third composition of the present invention are according to the general formula where R 9 is a saturated or unsaturated, branched or straight alkyl chain with 8-22 C atoms or R 13 CONH(CH 2 ) n where R 13 is saturated or unsaturated, branched or straight alkyl chain with 7-21 C atoms and n has value of 1 - 4, or R 14 CO O(CH 2 ) n where R 14 is saturated or unsaturated, branched or straight alkyl chain with 7-21 C atoms and n has value of 1 - 4, and R 10 is unsaturated or saturated, branched or straight alkyl chain with 1 - 22 C atoms or R 13 CONH(CH 2 ) n or R 14 COO(CH 2 ) n where R 13 , R 14 and n are same as above.
  • R 11 and R 12 are lower alkyl chain with 1 to 4 carbon atoms, and X is anion such as chloride, bromide, methosulfate.
  • Typical examples of those ingredients are cetyltrimethyl ammonium chloride, steartrimonium chloride, behentrimonium chloride, stearamidopropyl trimonuim chloride, dioleoylethyl dimethyl ammonium methosulfate, dioleoylethyl hydroxyethylmonium methosulfate.
  • Amido amines may as well be used as a conditioning cationic surfactant in the compositions of the present invention.
  • Typical non-limiting example is stearamidopropylamine known with a trade name Tego Amid S18 from Degussa and behenamidopropyl dimethyl amine available under the trade name Amidet APA 22 from Kao Chemicals.
  • Oily substances are selected from such as silicone oils, volatile or non-volatile, natural and synthetic oils.
  • silicone oils those can be added to the compositions include dimethicone, dimethiconol, polydimethylsiloxane, DC fluid ranges from Dow Corning, arylated silicones such as phenyl trimethicone or any other silicone with up to 5 aryl, preferably phenyl, group in its molecule, natural oils such as olive oil, almond oil, avocado oil, wheatgerm oil, ricinus oil and the synthetic oils, such as mineral oil, isopropyl myristate, palmitate, stearate and isostearate, oleyl oleate, isocetyl stearate, hexyl laurate, dibutyl adipate, dioctyl adipate, myristyl myristate and oleyl erucate.
  • compositions according to the invention may also comprise further conditioning substances such as protein hydrolyzates and polypeptides, e.g., keratin hydrolyzates, collagen hydrolyzates of the type “Nutrilan R " or elastin hydrolyzates, as well as also in particular plant protein hydrolyzates, optionally, cationized protein hydrolyzates, e.g., "Gluadin R ".
  • protein hydrolyzates and polypeptides e.g., keratin hydrolyzates, collagen hydrolyzates of the type "Nutrilan R " or elastin hydrolyzates
  • plant protein hydrolyzates e.g., cationized protein hydrolyzates, e.g., "Gluadin R ".
  • Typical concentration range for any of those conditioners, non-ionic compounds, oil or oil like substances, cationic polymers, silicon oil and derivatives and cationic surfactants is in the range of 0.01 - 10% by weight, preferably 0.01 - 7.5% by weight, more preferably 0.05 - 5% and most preferably 0.1 - 5% by weight calculated to the total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • the third composition in the form of an emulsion, it comprises as an emulsion base at least one fatty alcohol or mixture of fatty alcohols with the chain length of 14 to 22 C atoms.
  • suitable fatty alcohols without limiting the choice, are myristyl alcohol, cetyl alcohol, stearyl alcohol, behenyl alcohol and cetostearyl alcohol.
  • cetostearyl alcohol well known with its trade name Lanette O or as Lanette N in mixture with sodium cetearyl sulfate from Cognis.
  • the concentration of fatty alcohol(s) may be in the range from 0.5 to 20%, preferably 1 to 15% by weight, calculated to total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • the third composition according to present invention may comprise surfactants selected from anionic, nonionic, amphoteric (or zwiterionic) and/or cationic surfactants or their mixtures as emulsifier or solubilizer.
  • Cationic surfactants are as well used as hair conditioners as mentioned above.
  • Anionic surfactants suitable within the scope of the invention are in principal known from the cleansing compositions
  • anionic surfactants of the sulfate, sulfonate, carboxylate and alkyl phosphate type for example, the known C 10 -C 18 -alkyl sulfates, and in particular the respective ether sulfates, for example, C 12 -C 14 -alkyl ether sulfate, lauryl ether sulfate, especially with 1 to 4 ethylene oxide groups in the molecule, monoglyceride (ether) sulfates, fatty acid amide sulfates obtained by ethoxylation and subsequent sulfatation of fatty acid alkanolamides, and the alkali salts thereof, as well as the salts of long-chain mono- and dialkyl phosphates.
  • ether sulfates for example, C 12 -C 14 -alkyl ether sulfate, lauryl ether sulfate, especially with 1 to 4 ethylene oxide groups in the molecule
  • Additional anionic surfactants useful within the scope of the invention are ⁇ -olefin sulfonates or the salts thereof, and in particular alkali salts of sulfosuccinic acid semiesters, for example, the disodium salt of monooctyl sulfosuccinate and alkali salts of long-chain monoalkyl ethoxysulfosuccinates.
  • Suitable surfactants of the carboxylate type are alkyl polyether carboxylic acids and the salts thereof as well as alkyl amido polyether carboxylic acids and salts thereof.
  • Such products have been known for some time and are on the market, for example, under the trade name “AKYPO ® " and "AKYPO-SOFT ® ".
  • anionic surfactants are also C 8 -C 22 -acyl aminocarboxylic acids or the water-soluble salts thereof.
  • N-lauroyl glutamate in particular as sodium salt
  • N-lauroyl sarcosinate N-C 12 -C 18 -acyl asparaginic acid
  • N-myristoyl sarcosinate N-oleoyl sarcosinate
  • N-lauroyl methylalanine N-lauroyl lysine
  • N-lauroyl aminopropyl glycine preferably in form of the water-soluble alkali or ammonium, in particular the sodium salts thereof, preferably in admixture with the above-named anionic surfactants.
  • Further surfactants in the third composition according to the invention may be nonionic surfactants which are one of the preferred emulsifying surfactant within the scope of present invention.
  • nonionic surfactants are, for example, long-chain fatty acid mono- and dialkanolamides, such as coco fatty acid mono- or diethanolamide and myristic fatty acid mono or diethanolamide, stearic acid mono or diethanolamide.
  • Further nonionic surfactants suited are alkyl polyglucosides with an alkyl group of 8 to 18 carbon atoms, and with 1 to 5 glucoside units.
  • nonionic surfactants are, for example, the various sorbitan esters, such as polyethylene glycol sorbitan stearic acid ester, fatty acid polyglycol esters or poly-condensates of ethyleneoxide and propyleneoxide, as they are on the market, for example, under the trade name "Pluronics R ", as well as fatty alcohol ethoxylates.
  • Further nonionic surfactants preferred in the dyeing compositions according to invention are C 10 -C 22 -fatty alcohol ethoxylates.
  • C 10 -C 22 -fatty alcohol ethers the alkyl polyglycol ethers known by the generic terms “Laureth”, “Myristeth”, “Oleth”, “Ceteth”, “Deceth”, “Steareth” and “Ceteareth” according to the CTFA nomenclature, including addition of the number of ethylene oxide molecules, e.g., "Laureth-16”: The average degree of ethoxylation thereby ranges between about 2.5 and about 25, preferably about 10 and about 20.
  • the dyeing compositions according to the invention can also contain amphoteric or zwitterionic surfactants.
  • amphoteric or zwitterionic surfactants Useful as such are in particular the various known betaines such as alkyl betaines, fatty acid amidoalkyl betaines and sulfobetaines, for example, lauryl hydroxysulfobetaine; long-chain alkyl amino acids, such as cocoaminoacetate, cocoaminopropionate and sodium cocoamphopropionate and -acetate have also proven suitable.
  • Cationic surfactants mentioned above as conditioner and especially those with single long alkyl chain such as cetrimonium chloride and behentrimonium chloride are also suitable emulsifiers according to present invention.
  • the concentration of one or more emulsifiers in the third compositions may be in the range from 0.1 to 15%, preferably 0.5 to 10% by weight, calculated to total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • the third composition according to the present invention can contain organic solvent.
  • organic solvents are benzyloxy ethanol, benzyl alcohol, phenoxy ethanol, phenoxy isopropanol, methyl phenoxy ethanol, benzyl glycerol, N-benzyl formide, N-methyl pyrrolidone, N-ethyl pyrrolidone, cinnamyl alcohol, phenethyl alcohol, p-methyl benzyl alcohol, butyl cellosolve, methyl carbitol, ethyl carbitol, propyl carbitol, butyl carbitol, diethyleneglycol, diethyl ether and dipropyleneglycol diethyl ether.
  • concentration of those solvents can be in the range from 0.5% to 10%, preferably 0.5 - 5% by weight calculated to the total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • the third composition can contain one or more thickening agents.
  • the thickening agents disclosed for water free bleaching and/or highlighting compositions are also suitable for the third composition at the above given concentration ranges.
  • ceramide type of compounds according to general formula wherein R 20 and R 21 are independent from each other alkyl- or. alkenyl group with 10 to 22 carbon atoms, R 22 is alkyl or hydroxyl alkyl with 1 to 4 carbon atoms group and n is a number between 1 to 6, preferably 2 or 3.
  • Preferred compound according to the above chemical structure is cetyl-PG-hydroxyethylpalmitamide. Concentration of ceramide type of compounds ranges from 0.01 to 2%, preferably 0.01 to 1% by weight calculated to total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • ubichinone type of compounds according to general formula wherein n is a number from 1 to 10. Concentration of ubichinone can vary between 0.001 % and 10 % by weight, calculated to the total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • the third composition may as well comprise UV filters of oil soluble, non-ionic, ones and/or as well those of water soluble and mainly of anionic character.
  • Non-limiting examples are Benzophenone-1 Benzophenone-2, Benzophenone-3, Benzophenone-7, Benzophenone-6, Benzophenone-8, octylmethoxy cinnamate, homosalat to those of oil soluble ones and Benzophenone-4, benzophenone-9 to those anionic water soluble ones.
  • Concentration of UV filters may be in the range of 0.05 to 5%, preferably 0.1 to 2.5% and more preferably 0.1 to 1% by weight calculated to total composition prior to mixing with oxidizing and bleaching and/or highlighting composition.
  • Conditioning agents preferred are the ones mentioned above as oily lipophilic ingredients such as natural, synthetic and mineral oils and cationic compounds such as quaternary ammonium surfactants and cationic polymer disclosed above as well.
  • the third composition comprises at least one direct dye.
  • Suitable direct dyes are anionic, cationic and non-ionic nitro dyes.
  • Suitable anionic direct dyes in aqueous composition are Acid Black 1, Acid Blue 1, Acid Blue 3, Food Blue 5, Acid Blue 7, Acid Blue 9, Acid Blue 74, Acid Orange 3, Acid Orange 6, Acid Orange 7, Acid Orange 10, Acid Red 1, Acid Red 14, Acid Red 18, Acid Red 27, Acid Red 50, Acid Red 52, Acid Red 73, Acid Red 87, Acid Red 88, Acid Red 92, Acid Red 155, Acid Red 180, Acid Violet 9, Acid Violet 43, Acid Violet 49, Acid Yellow 1, Acid Yellow 23, Acid Yellow 3, Food Yellow No. 8, D&C Brown No. 1, D&C Green No. 5, D&C Green No. 8, D&C Orange No. 4, D&C Orange No. 10, D&C Orange No. 11, D&C Red No. 21, D&C Red No. 27, D&C Red No.
  • D&C Violet 2 D&C Yellow No. 7, D&C Yellow No. 8, D&C Yellow No. 10, FD&C Red 2, FD&C Red 40, FD&C Red No. 4, FD&C Yellow No. 6, FD&C Blue 1, Food Black 1, Food Black 2, Disperse Black 9 and Disperse Violet 1 and their alkali metal salts such as sodium, potassium.
  • the most preferred anionic dyestuffs are Acid Red 52, DC Violet 2, DC Red 33, DC Orange 4, DC Red 27 and DC Yellow 10.
  • Suitable cationic dyes in aqueous composition are in principal those available on the market for cosmetic hair colouring applications.
  • PCT application WO 95/15144 of Ciba-Geigy AG Some examples to those are Basic Blue 6, Basic Blue 7, Basic Blue 9, Basic Blue 26, Basic Blue 41, Basic Blue 99, Basic Brown 4, Basic Brown 16, Basic Brown 17, Natural Brown 7, Basic Green 1, Basic Red 2, Basic Red 12 Basic Red 22, Basic Red 76, Basic Violet 1, Basic Violet 2, Basic Violet 3, Basic Violet 10, Basic Violet 14, Basic Yellow 57, Basic red 51, Basic Yellow 87 and Basic Orange 31.
  • the most preferred ones are Basic red 51, Basic Yellow 87 and Basic Orange 31 sold by CIBA.
  • aqueous compositions of the present invention may comprise neutral dyes (HC dyes), so called nitro dyes for shading purposes.
  • HC dyes neutral dyes
  • Some examples to those are: HC Blue No.2, HC Blue No.4, HC Blue No.5, HC Blue No.6, HC Blue No.7, HC Blue No.8, HC Blue No.9, HC Blue No.10, HC Blue No.11, HC Blue No.12, HC Blue No.13, HC Brown No.1, HC Brown No.2, HC Green No.1, HC Orange No.1, HC Orange No.2, HC Orange No.3, HC Orange No.5, HC Red BN, HC Red No.1, HC Red No.3, HC Red No.7, HC Red No.8, HC Red No.9, HC Red No.10, HC Red No.11, HC Red No.13, HC Red No.54, HC Red No.14, HC Violet BS, HC Violet No.1, HC Violet No.2, HC
  • Plant dyestuffs can also be used alone or in combination with synthetic direct-acting dyestuffs, for example henna (red or black), alkanna root, laccaic acid, indigo, logwood powder, madder root and rhubarb powder, etc.
  • henna red or black
  • alkanna root laccaic acid
  • indigo indigo
  • the third composition may comprise one or more direct dye at a concentration of 0.1 to 7.5% by weight calculated to the total composition prior to mixing with bleaching and oxidizing compositions mentioned above.
  • the third composition can also comprise mixture of several direct dyes i.e. an anionic, a cationic and/or a nonionic ones. In such a case the dyes may be mixed at any ratio with each other.
  • the above mentioned direct dyes of cationic, anionic and nonionic character can also be added into the water free bleaching and/or highlighting composition at the concentration given in the above paragraph.
  • the direct dyes of different characters can certainly be mixed as well.
  • pH of the aqueous third composition of the present invention may vary between 2 and 12, preferably 3 - 10, more preferably 4 to 8. pH is adjusted to the required pH by using monoethanolamine, triethanolamine, ammonia or its salts with acids such as ammonium chloride, ammonium sulphate, ammonium carbonate, ammonium bicarbonate, ammonium nitrate, or using alkaline solutions such as sodium hydroxide, potassium hydroxide and their respective salts with the known acids.
  • pH of the mixture of bleaching and/or highlighting composition, third composition and oxidizing lotion, ready to use composition may be in the range of 8 to 12, in particular between 9 and 11.
  • the mixing ratio of the bleaching and/or highlighting composition to third composition may vary between 10:1 to 1:1, preferably 8:1 to 2:1 and more preferably 5:1 to 3:1, all by weight, which may further mixed with an oxidizing lotion at a weight ratio of preferably 1:1.
  • the above ratios are valid when third composition does not comprise direct dye.
  • direct dye is contained in the third composition preferred mixing ratio is 1:1 which than mixed with oxidizing lotion.
  • Hair bleaching process is carried out as usual using the compositions of the present invention. Briefly, the mixture of water free composition, oxidizing lotion and optionally third compositions is prepared and applied onto dry hair and processed for 1 to 45 min and rinsed of from hair and shampooed, if necessary.
  • a substantially water free composition of the present invention is mixed homogeneously with an aqueous composition comprising at least one oxidizing agent and optionally a third composition comprising at least one at least one hair conditioning agent and/or a direct dye and applied onto hair and after processing 1 to 45 min rinsed off from hair.
  • bleaching and/or highlighting composition of the present invention is firstly mixed with an oxidizing agent and applied onto hair and left 5 to 20 min and afterwards without rinsing off the third composition comprising at least one direct dye is applied onto hair and additionally processed for 5 to 30 min and rinsed off from hair and shampooed, if necessary.
  • bleaching and/or highlighting composition of the present invention is firstly mixed with an oxidizing agent and applied onto hair and left 5 to 45 min and afterwards rinsed off from hair and subsequently in the second step dyeing composition is applied onto hair and additionally processed for 5 to 45 min and rinsed off from hair and shampooed, if necessary.
  • composition of the present invention can contain additional ingredients such as preservatives, chelating agents, fragrance and substances customarily used in cosmetic bleaching and colouring compositions of keratin fibres, especially hair.
  • the above composition is prepared by combining all powder components together and mixing until homogeneity in a suitable mixer.
  • the water free bleaching composition was mixed with an oxidizing composition of the following composition at a weight ratio of water free powder to oxidizing lotion 1:2.
  • the composition was applied onto hair and processed at room temperature for 30 min and rinsed off and hair was dried.
  • the hair was homogeneously bleached.
  • the above composition was tested in a half side test for its performance on bleaching with 10 volunteers having shoulder length hair.
  • a comparative composition a composition without Sodium Gluconate but with 15.5% by weight diatomaceous earth was prepared.
  • Bleaching composition was prepared by mixing above water free composition with oxidizing lotion of example 1 at a weight ratio of 1:2 (powder to lotion). Approximately 30 g of each was applied onto hair and processed for 30 min at ambient temperature. Afterwards bleaching composition was rinsed off from hair and shampooed ones and dried with a hair drier.
  • Bleaching and colouring in a single process was carried out using the bleaching composition of example 1, dyeing composition according to the composition below and an oxidizing lotion composition of example 1, however with 6% hydrogen peroxide content instead of 9%.
  • the bleaching composition of example 2 dyeing composition of above and oxidizing lotion of example 1 were mixed at a weight ratio of 1:1:1 and was applied onto parts of hair (streak) and left 30 min at 40°C and rinsed off with water and shampooed. Intensive highlighted red streaks were obtained.
  • Cetrimonium chloride 1.0 Hydroxyethylcellulose 1.0 Cetearyl alcohol 5.0 Hydrolysed silk 1.0 Fragrance q.s. Preservative q.s. Citric acid q.s. to pH 5.0 Water to 100
  • Water free bleaching composition of example 2 is mixed with above composition and with oxidizing lotion of example 1 at a weight ratio of 1:1.9:0.1 (water free composition: oxidizing lotion: the third composition).
  • the resulting composition was tested against a bleaching composition of Example 2. It was observed that the half side bleached with a composition mixed with third composition is much more cared interms of combability, shine and softness.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Claims (15)

  1. Composition décolorante et/ou éclaircissante pour les fibres kératiniques, en particulier pour les cheveux humains, à base d'au moins un composé ayant un effet décolorant et/ou éclaircissant à une concentration d'au moins 5 % en poids, calculée par rapport à la composition totale, caractérisée par le fait qu'elle comprend de l'acide gluconique et/ou ses sels en tant qu'agent chélateur, dans laquelle aucune eau supplémentaire n'est introduite dans la composition autre que l'eau liée qui peut atteindre 1% en poids, calculée par rapport à la composition totale, les compositions composées de citrate de sodium (15-30%), de silicate de sodium (15-30%), de percarbonate de sodium (15-30%), de carbonate de sodium (5-15%), de gluconate de sodium (5-15%) et de tensioactifs végétaux non ioniques (<5%) étant exclues du champ d'application de la présente directive.
  2. Composition selon la revendication 1 caractérisée par le fait qu'elle comprend au moins un composé ayant un effet blanchissant et/ou éclaircissant à une concentration comprise entre 5 et 80% en poids, calculée par rapport à la composition totale.
  3. Composition selon les revendications 1 et 2 caractérisée par le fait qu'elle comprend au moins un sel d'ammonium.
  4. Composition selon les revendications 1 et 2 caractérisée par le fait que l'agent chélateur est un sel gluconique choisi parmi les sels de sodium, de potassium et d'ammonium.
  5. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait que l'agent chélateur est compris dans une concentration allant de 0,01 à 10 % en poids calculé par rapport au total de la composition.
  6. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait qu'elle comprend de l'huile de silicone et/ou de l'huile minérale et/ou de l'huile naturelle comme ingrédient lipophile.
  7. Composition selon l'une quelconque des revendications précédentes caractérisée en ce qu'elle comprend au moins un ingrédient lipophile à une concentration de 1 à 50% en poids calculé par rapport à la composition totale.
  8. Composition selon l'une quelconque des revendications précédentes caractérisée en ce qu'elle comprend un polymère.
  9. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait qu'elle comprend au moins un polymère cationique.
  10. Composition selon l'une quelconque des revendications précédentes caractérisée en ce qu'elle comprend un composé ayant deux liaisons amide dans sa structure est un composé selon la structure générale
    Figure imgb0016
    où R1 est une chaîne alkyle linéaire ou ramifiée, saturée ou insaturée, de 1 à 12 atomes de carbone, qui peut être substituée par des groupes hydroxy et/ou alcoxy, R2 est une chaîne alkyle linéaire ou ramifiée de 1 à 5 atomes de carbone, et R3 une chaîne alkyle linéaire ou ramifiée, saturée ou insaturée, de 1 à 22 atomes de carbone.
  11. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait qu'elle comprend au moins un mica synthétique recouvert d'oxyde(s) métallique(s) ayant une distribution granulométrique en volume comprise entre 1 et 750 µm.
  12. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait qu'elle comprend un ou plusieurs sels de calcium et/ou de magnésium.
  13. Composition selon l'une quelconque des revendications précédentes caractérisée par le fait qu'elle comprend au moins un agent alcalinisant.
  14. Kit de décoloration et/ou de mise en valeur des cheveux humains comprenant
    a- une composition selon les revendications 1 à 13,
    b- une composition aqueuse comprenant au moins un agent oxydant
    c- éventuellement, une troisième composition, de préférence aqueuse, comprenant au moins un agent de conditionnement capillaire et/ou un colorant direct.
  15. Procédé de décoloration des cheveux dans lequel une composition selon la revendication 1 à 13 est mélangée de façon homogène avec une composition aqueuse comprenant au moins un agent oxydant et éventuellement une troisième composition comprenant au moins un agent de conditionnement capillaire et/ou un colorant direct et appliquée sur les cheveux et après traitement 1 à 45 min rincée des cheveux.
EP11807932.6A 2010-12-28 2011-12-23 Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels Active EP2658510B2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11807932.6A EP2658510B2 (fr) 2010-12-28 2011-12-23 Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10016113A EP2471502A1 (fr) 2010-12-28 2010-12-28 Composition de blanchiment comprenant un acide polyhydroxy carboxylique
EP11807932.6A EP2658510B2 (fr) 2010-12-28 2011-12-23 Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels
PCT/EP2011/073998 WO2012089683A1 (fr) 2010-12-28 2011-12-23 Composition de décoloration comprenant un acide polyhydroxycarboxylique

Publications (3)

Publication Number Publication Date
EP2658510A1 EP2658510A1 (fr) 2013-11-06
EP2658510B1 EP2658510B1 (fr) 2018-07-25
EP2658510B2 true EP2658510B2 (fr) 2025-04-02

Family

ID=43901574

Family Applications (2)

Application Number Title Priority Date Filing Date
EP10016113A Withdrawn EP2471502A1 (fr) 2010-12-28 2010-12-28 Composition de blanchiment comprenant un acide polyhydroxy carboxylique
EP11807932.6A Active EP2658510B2 (fr) 2010-12-28 2011-12-23 Composition de blanchiment comprenant de l'acide gluconique et/ou ses sels

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP10016113A Withdrawn EP2471502A1 (fr) 2010-12-28 2010-12-28 Composition de blanchiment comprenant un acide polyhydroxy carboxylique

Country Status (3)

Country Link
US (1) US9233058B2 (fr)
EP (2) EP2471502A1 (fr)
WO (1) WO2012089683A1 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2883572B1 (fr) * 2013-12-13 2018-10-17 Kao Corporation Composition de blanchiment/d'éclaircissement des cheveux
EP2883571B1 (fr) * 2013-12-13 2018-09-12 Kao Corporation Composition de blanchiment/d'éclaircissement des cheveux
DE102015208788A1 (de) 2015-05-12 2016-11-17 Henkel Ag & Co. Kgaa Mittel zur schonenden oxidativen Aufhellung von keratinhaltigen Fasern
EP3346973B1 (fr) * 2015-09-08 2020-09-23 Kao Germany GmbH Composition pour la teinture oxydative des cheveux
EP3346972B1 (fr) * 2015-09-08 2021-05-26 Kao Germany GmbH Procédé de traitement des cheveux
US10632053B2 (en) * 2015-09-08 2020-04-28 Kao Germany Gmbh Process for bleaching hair
WO2017041906A1 (fr) * 2015-09-08 2017-03-16 Kao Germany Gmbh Méthode de traitement capillaire
DE102018123454A1 (de) * 2018-09-24 2020-03-26 Henkel Ag & Co. Kgaa Reduzierte Haarschädigung während der Blondierung durch Einsatz von einem biologisch abbaubaren Komplexbildner
DE102018123526A1 (de) * 2018-09-25 2020-03-26 Henkel Ag & Co. Kgaa Reduzierte Haarschädigung während der Blondierung durch Einsatz von einem biologisch abbaubaren Komplexbildner
DE102019105162A1 (de) * 2018-12-28 2020-07-02 Henkel Ag & Co. Kgaa Verdickungssystem in einem Percarbonat haltigen Blondiermittel
FR3157153A1 (fr) * 2023-12-20 2025-06-27 L'oreal Composition comprenant un (bi)carbonate, un silicate et un corps gras dans une teneur particulière
FR3159317A1 (fr) * 2024-02-19 2025-08-22 L'oreal Procédé de décapage de la couleur artificielle des fibres kératiniques à partir de plusieurs types de composés peroxygénés, une composition et un kit

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19705875C1 (de) 1997-02-15 1998-04-02 Wella Ag Mittel zum oxidativen Färben von Haaren
JP2002205924A (ja) 2001-01-09 2002-07-23 Kao Corp 染毛剤
FR2852834A1 (fr) 2003-03-25 2004-10-01 Oreal Composition oxydante comprenant des acides hydroxycarboxyliques et leurs sels comme agents complexants pour la coloration, la decoloration ou la deformation permanente des fibres keratiniques

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4207475A1 (de) 1992-03-10 1993-09-16 Goldwell Ag Mittel zum blondieren von menschlichen haaren und verfahren zu dessen herstellung
EP0609796B1 (fr) 1993-02-01 1998-12-02 GOLDWELL GmbH Composition pour décoloré des cheveux humains
DE69424100T2 (de) 1993-08-10 2000-10-12 Kao Corp Organopolysiloxane und ein Verfahren zum Haarfestigen unter Verwendung derselben
TW325998B (en) 1993-11-30 1998-02-01 Ciba Sc Holding Ag Dyeing keratin-containing fibers
JPH08175940A (ja) 1994-12-27 1996-07-09 Shiyuwarutsukofu Kk 染毛方法及びそれに用いる染毛剤組成物
DE19545853A1 (de) 1995-12-08 1997-06-12 Wella Ag Mittel zum Bleichen von Haaren
WO2002089754A1 (fr) 2001-03-20 2002-11-14 The Procter & Gamble Company Compositions convenant pour le traitement des cheveux comprenant des chélatants, et procédé pour réduire la détérioration des cheveux par oxydation
US20040253283A1 (en) * 2003-03-25 2004-12-16 L'oreal S.A. Composition for treating keratinous materials, comprising a hydroxycarboxylic acid and a protective and/or conditioning agent
US20050011017A1 (en) * 2003-03-25 2005-01-20 L'oreal S.A. Oxidizing composition comprising hydroxycarboxylic acids and salts thereof as complexing agents for dyeing, bleaching or permanently reshaping keratin fibres
FR2852836B1 (fr) * 2003-03-25 2008-02-15 Oreal Utilisation d'acides hydroxycarboxyliques et de leurs sels comme agents complexants dans des compositions reductrices pour la decoloration ou la deformation permanente de fibres keratiniques
FR2852832B1 (fr) * 2003-03-25 2008-06-27 Oreal Composition de coloration pour fibres keratiniques comprenant un acide hydroxycarboxilique ou un sel, composition prete a l'emploi la comprenant, procede de mise en oeuvre et dispositif
US20050142084A1 (en) 2003-12-29 2005-06-30 Sanjoy Ganguly Cosmetic compositions containing nacreous pigments of large sized synthetic mica
EP2055296B1 (fr) 2007-11-02 2012-09-05 Kao Germany GmbH Composition de blanchiment
EP2191812A1 (fr) * 2008-11-27 2010-06-02 KPSS-Kao Professional Salon Services GmbH Composition de blanchiment/balayage
EP2246097A1 (fr) * 2009-04-27 2010-11-03 KPSS-Kao Professional Salon Services GmbH Composition de blanchiment

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19705875C1 (de) 1997-02-15 1998-04-02 Wella Ag Mittel zum oxidativen Färben von Haaren
JP2002205924A (ja) 2001-01-09 2002-07-23 Kao Corp 染毛剤
FR2852834A1 (fr) 2003-03-25 2004-10-01 Oreal Composition oxydante comprenant des acides hydroxycarboxyliques et leurs sels comme agents complexants pour la coloration, la decoloration ou la deformation permanente des fibres keratiniques

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
BIO SPECTRA: "Phosphate-Free Automatic Dishwashing Tablets", MINTEL GNPD EINTRAG NUMMER 1418505 ZU DEM GESCHIRRSPÜLMITTEL ''ATTITUDE, 31 October 2010 (2010-10-31), XP055585020, Retrieved from the Internet <URL:http://www.gnpd.com/sinatra/recordpage/1418505>

Also Published As

Publication number Publication date
EP2658510A1 (fr) 2013-11-06
EP2471502A1 (fr) 2012-07-04
EP2658510B1 (fr) 2018-07-25
WO2012089683A1 (fr) 2012-07-05
US20130284199A1 (en) 2013-10-31
US9233058B2 (en) 2016-01-12

Similar Documents

Publication Publication Date Title
EP2658510B2 (fr) Composition de blanchiment comprenant de l&#39;acide gluconique et/ou ses sels
EP2358335B1 (fr) Composition de blanchiment/éclaircissement
EP2424619B1 (fr) Composition de blanchiment
EP2358441B1 (fr) Composition décolorante et éclaircissante
US9278057B2 (en) Bleaching/highlighting composition containing calcium salts
EP2516012B1 (fr) Composition de décoloration
EP2670381B1 (fr) Composition décolorante
US20170000700A1 (en) Bleaching/highlighting composition
US8617255B2 (en) Bleaching composition comprising magnesium salt

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20130711

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20160425

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

RIC1 Information provided on ipc code assigned before grant

Ipc: A61K 8/365 20060101ALI20180129BHEP

Ipc: A61Q 5/08 20060101ALI20180129BHEP

Ipc: A61K 8/23 20060101ALI20180129BHEP

Ipc: A61K 8/22 20060101AFI20180129BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20180309

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1020980

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180815

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602011050404

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20180725

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1020980

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180725

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181125

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181026

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181025

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181025

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602011050404

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

26 Opposition filed

Opponent name: HENKEL AG & CO. KGAA

Effective date: 20190416

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181223

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20181231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181223

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181223

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20200113

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180725

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20111223

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180725

RDAF Communication despatched that patent is revoked

Free format text: ORIGINAL CODE: EPIDOSNREV1

PLBP Opposition withdrawn

Free format text: ORIGINAL CODE: 0009264

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230426

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

PLAY Examination report in opposition despatched + time limit

Free format text: ORIGINAL CODE: EPIDOSNORE2

PLBC Reply to examination report in opposition received

Free format text: ORIGINAL CODE: EPIDOSNORE3

PLAY Examination report in opposition despatched + time limit

Free format text: ORIGINAL CODE: EPIDOSNORE2

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20241216

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20241218

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20241218

Year of fee payment: 14

PUAH Patent maintained in amended form

Free format text: ORIGINAL CODE: 0009272

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT MAINTAINED AS AMENDED

27A Patent maintained in amended form

Effective date: 20250402

AK Designated contracting states

Kind code of ref document: B2

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: DE

Ref legal event code: R102

Ref document number: 602011050404

Country of ref document: DE